幽灵蛋白
肌动蛋白
细胞骨架
生物物理学
化学
异源的
膜
肌动蛋白细胞骨架
细胞生物学
EPB41
锚定
索马
生物
蛋白质丝
肌动蛋白重塑
作者
Nicholas P. Boyer,Rohan Sharma,Theresa Wiesner,Christopher Parperis,Antoine Delamare,Florence Pelletier,Nicolas Jullien,A. M. Pethe D.A.Bhatt,Leonardo A Parra‐Rivas,Patrick J. Kearney,Farbod Shavarebi,Christophe Leterrier,Subhojit Roy
出处
期刊:iScience
[Cell Press]
日期:2025-12-16
卷期号:29 (1): 114454-114454
被引量:1
标识
DOI:10.1016/j.isci.2025.114454
摘要
In axons, α/β-spectrins, adducin, and actin filaments assemble into a lattice underneath the plasma membrane, but the mechanistic events leading to this membrane-associated periodic skeleton (MPS) are unclear. Visualizing MPS-components in developing axons, we found distal focal patches containing spectrins and adducin (but sparse actin filaments) with biophysical properties reminiscent of biomolecular condensation. Overexpressing spectrin repeats - constituents of α/β-spectrins - in heterologous cells triggered condensate formation, and preventing the association of βII-spectrin with actin filaments or membranes also facilitated condensation. Introducing a stretch of spectrin-repeats in neurons before MPS establishment triggered ectopic condensate-like structures in the soma and disrupted the axonal lattice, advocating a functional role for biomolecular condensation. We propose a condensation-assembly model where spectrin-repeats trigger focal phase separated condensates, providing a nidus for MPS assembly that recruits actin filaments to ultimately generate the stable lattice. Our overall model is supported by recent studies showing phase-separation via coiled-coil domains and recruitment/polymerization of actin by other condensate-forming proteins.
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